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Lower risk Drug recall · FDA · Published March 8, 2023

Pfizer MEKTOVI tablets: Incorrect expiration date on labels

Pfizer recalls 15 mg MEKTOVI tablets due to incorrect expiration date on labels. The correct expiration is February 2025, but labels show March 2026. This affects prescription medication.

🇺🇸 FDA recall #D-0532-2023DrugPfizer ›
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Recalling firmPfizer Inc.235 East 42nd Street · New York, NY 10017-5703
✎ GovInfoNow plain-language explainer

Pfizer is recalling 15 mg MEKTOVI tablets because the labels show an incorrect expiration date (March 2026 instead of February 2025). This could lead to medication safety issues if the expired product is used. Read more at govinfonow.com/recall/33828-pfizer-mektovi-tablets-incorrect-expiration-date-on-labels.

Source Summary by GovInfoNow · govinfonow.com/recall/33828-pfizer-mektovi-tablets-incorrect-expiration-date-on-labels · Updated August 18, 2026 · FDA enforcement record: FDA #D-0532-2023

Cite this page

“Pfizer MEKTOVI tablets: Incorrect expiration date on labels.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/33828-pfizer-mektovi-tablets-incorrect-expiration-date-on-labels. Based on FDA recall #D-0532-2023 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0532-2023%22&limit=1).

The FDA announced on March 8, 2023, that Pfizer Inc. recalls MEKTOVI (binimetinib) tablets due to incorrect labeling stating an expiration date of March 2026 instead of the correct February 2025. The agency identified the hazard as a potential risk from using medication past its actual expiration date.

How to tell if you have it

  • Brand: Pfizer
  • Product: MEKTOVI (binimetinib) tablets, 15 mg
  • Packaging: 180-count bottle
  • NDC: 70255-010-02
  • Lot Code: W054586A
  • Incorrect Expiry Date on Label: March 2026
  • Correct Expiry Date: February 2025
  • Quantity: 1,926 bottles
  • Distribution: Nationwide in the USA

The hazard

The carton and bottle labels state an expiry date of March 2026, but the correct expiration date is February 2025. The FDA classified this as a Class III recall.

Context

GovInfoNow's records show Pfizer Inc. has 71 other recalls on record since November 26, 2012. Recent Pfizer recalls include a sodium bicarbonate injection recall due to lack of sterility assurance on August 4, 2025, and a Bicillin L-A injectable suspension recall for particulate risk on July 10, 2025. Other recent recalls of similar products include OurPharma Fentanyl Injection Recall: IV Bag Expiry Discrepancy (September 3, 2026), Premier Dental Products: Incorrect Expiration Date on Ferric Subsulfate Solution (April 14, 2026), and Kirkman Lidocaine Cream Recall: Stability Issues May Affect Expiry Date (February 18, 2026).

How to tell if you have this one

Check for MEKTOVI tablets (15 mg, 180-count bottle) with NDC 70255-010-02. Labels show expiration date March 2026 instead of February 2025.

  • Brand
    Pfizer
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Labels

    Look for the expiration date on the label; it should be February 2025, not March 2026.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 42 days after the firm started it.

1. Firm started the recall: Mar 8, 202312. FDA classified it Class III: Apr 13, 202323. Published in FDA’s Enforcement Report: Apr 19, 202332023
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0532-2023 (March 8, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0532-2023 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA